Regulation of cell death protease caspase-9 by phosphorylation

被引:2619
作者
Cardone, MH
Roy, N
Stennicke, HR
Salvesen, GS
Franke, TF
Stanbridge, E
Frisch, S
Reed, JC
机构
[1] Burnham Inst, Program Apoptosis & Cell Death Res, La Jolla, CA 92037 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] Columbia Univ, Dept Pharmacol, New York, NY 10032 USA
[4] Univ Calif Irvine, Dept Microbiol & Mol Genet, Irvine, CA 92697 USA
关键词
D O I
10.1126/science.282.5392.1318
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Caspases are intracellular proteases that function as initiators and effectors of apoptosis. The kinase Akt and p21-Ras, an Akt activator, induced phosphorylation of pro-caspase-9 (pro-Casp9) in cells. Cytochrome c-induced proteolytic processing of pro-Casp9 was defective in cytosolic extracts from cells expressing either active Ras or Akt. Akt phosphorylated recombinant Casp9 in vitro on serine-196 and inhibited its protease activity. Mutant pro-Casp9(Ser196Ala) was resistant to Akt-mediated phosphorylation and inhibition in vitro and in cells, resulting in Akt-resistant induction of apoptosis. Thus, caspases can be directly regulated by protein phosphorylation.
引用
收藏
页码:1318 / 1321
页数:4
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